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Ansuvimab: First Approval
Ansuvimab (ansuvimab-zykl; EBANGA™) is a human monoclonal antibody developed by Ridgeback Biotherapeutics, which binds to the glycoprotein on Zaire ebolavirus (Ebola virus) to block its entry into host cells. Ansuvimab has been recently approved in the USA for the treatment of infection caused by Z....
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Springer International Publishing
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7983082/ https://www.ncbi.nlm.nih.gov/pubmed/33751449 http://dx.doi.org/10.1007/s40265-021-01483-4 |
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author | Lee, Arnold |
author_facet | Lee, Arnold |
author_sort | Lee, Arnold |
collection | PubMed |
description | Ansuvimab (ansuvimab-zykl; EBANGA™) is a human monoclonal antibody developed by Ridgeback Biotherapeutics, which binds to the glycoprotein on Zaire ebolavirus (Ebola virus) to block its entry into host cells. Ansuvimab has been recently approved in the USA for the treatment of infection caused by Z. ebolavirus in adult and paediatric patients, including in neonates born to a mother who is RT-PCR positive for Z. ebolavirus infection, following the results of the PALM phase II/III trial. This article summarizes the milestones in the development of ansuvimab leading to this first approval for the treatment of infections caused by Ebola virus in adults and paediatric patients. |
format | Online Article Text |
id | pubmed-7983082 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer International Publishing |
record_format | MEDLINE/PubMed |
spelling | pubmed-79830822021-03-23 Ansuvimab: First Approval Lee, Arnold Drugs AdisInsight Report Ansuvimab (ansuvimab-zykl; EBANGA™) is a human monoclonal antibody developed by Ridgeback Biotherapeutics, which binds to the glycoprotein on Zaire ebolavirus (Ebola virus) to block its entry into host cells. Ansuvimab has been recently approved in the USA for the treatment of infection caused by Z. ebolavirus in adult and paediatric patients, including in neonates born to a mother who is RT-PCR positive for Z. ebolavirus infection, following the results of the PALM phase II/III trial. This article summarizes the milestones in the development of ansuvimab leading to this first approval for the treatment of infections caused by Ebola virus in adults and paediatric patients. Springer International Publishing 2021-03-22 2021 /pmc/articles/PMC7983082/ /pubmed/33751449 http://dx.doi.org/10.1007/s40265-021-01483-4 Text en © Springer Nature Switzerland AG 2021 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | AdisInsight Report Lee, Arnold Ansuvimab: First Approval |
title | Ansuvimab: First Approval |
title_full | Ansuvimab: First Approval |
title_fullStr | Ansuvimab: First Approval |
title_full_unstemmed | Ansuvimab: First Approval |
title_short | Ansuvimab: First Approval |
title_sort | ansuvimab: first approval |
topic | AdisInsight Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7983082/ https://www.ncbi.nlm.nih.gov/pubmed/33751449 http://dx.doi.org/10.1007/s40265-021-01483-4 |
work_keys_str_mv | AT leearnold ansuvimabfirstapproval |